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具有先天功能的记忆表型CD8 + T细胞在缺乏活性Itk的情况下选择性发育。

Memory phenotype CD8+ T cells with innate function selectively develop in the absence of active Itk.

作者信息

Hu Jianfang, Sahu Nisebita, Walsh Elizabeth, August Avery

机构信息

Center for Molecular Immunology and Infectious Disease and Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Eur J Immunol. 2007 Oct;37(10):2892-9. doi: 10.1002/eji.200737311.

Abstract

T cells with a memory-like phenotype and possessing innate immune function have been previously identified as CD8(+)CD44(hi) cells. These cells rapidly secrete IFN-gamma upon stimulation with IL-12/IL-18 and are involved in innate responses to infection with Listeria monocytogenes. The signals regulating these cells are unclear. The Tec kinase Itk regulates T cell activation and we report here that a majority of the CD8(+) T cells in Itk null mice have a phenotype of CD44(hi) similar to memory-like innate T cells. These cells are observed in mice carrying an Itk mutant lacking the kinase domain, indicating that active Tec kinase signaling suppresses their presence. These cells carry preformed message for and are able to rapidly produce IFN-gamma upon stimulation in vitro with IL-12/IL-18, and endow Itk null mice the ability to effectively respond to infection with L. monocytogenes or exposure to lipopolysaccharides by secretion of IFN-gamma. Transfer of these cells rescues the ability of IFN-gamma null mice to reduce bacterial burden following L. monocytogenes infection, indicating that these cells are functional CD8(+)CD44(hi) T cells previously detected in vivo. These results indicate that active signals from Tec kinases regulate the development of memory-like CD8(+) T cells with innate function.

摘要

具有记忆样表型并拥有先天免疫功能的T细胞先前已被鉴定为CD8(+)CD44(hi)细胞。这些细胞在受到IL-12/IL-18刺激后会迅速分泌IFN-γ,并参与对单核细胞增生李斯特菌感染的先天反应。调节这些细胞的信号尚不清楚。Tec激酶Itk调节T细胞活化,我们在此报告,Itk基因敲除小鼠中的大多数CD8(+) T细胞具有与记忆样先天T细胞相似的CD44(hi)表型。在携带缺乏激酶结构域的Itk突变体的小鼠中观察到了这些细胞,这表明活跃的Tec激酶信号传导抑制了它们的存在。这些细胞携带预先形成的信息,并在体外受到IL-12/IL-18刺激时能够迅速产生IFN-γ,并赋予Itk基因敲除小鼠通过分泌IFN-γ有效应对单核细胞增生李斯特菌感染或接触脂多糖的能力。这些细胞的转移挽救了IFN-γ基因敲除小鼠在单核细胞增生李斯特菌感染后减轻细菌负荷的能力,表明这些细胞是先前在体内检测到的功能性CD8(+)CD44(hi) T细胞。这些结果表明,来自Tec激酶的活跃信号调节具有先天功能的记忆样CD8(+) T细胞的发育。

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